A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6371976



Internal ID21029529
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:136300801..136307200hg38UCSC Ensembl
chr3:136019643..136026042hg19UCSC Ensembl
Cytoband3q22.3
Allele length
AssemblyAllele length
hg386400
hg196400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18094927
Samples
Known GenesPCCB
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6371976
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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